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"TMS" was not a discovery, but a theory. It is also nothing more than a string of words that Dr. Sarno put together to describe the symptom of muscle pain resulting from muscle tension which he believed was from oxygen deprivation, which he theorized was caused by emotional distress and repression. Forty years ago in the early 1980s.TMS was discovered in relation to conditions like back pain,
I think they use a physical treatment (though maybe it's ultimately psychological?) of focusing on something else while walking, which helps rewire the brain's ability to walk as an automatic function...
It seems to me that although it's a physical practice, it's acknowledging the real cause of the problem (neuropathways), so is psychologically reinforcing the right thing.
Exactly!Of course doing some emotional/psychological work to look at what caused the neuropathways to end up like that in the first place, is going to help the symptoms not just shift to some other area once the brain is able to manage automatic movements again,
Well, look - this is highly individualized (as @Cactusflower has also said) and I think it depends a LOT on where someone is at in incorporating TMS knowledge and awareness and skills into their life. In my case, I was on my way to becoming housebound, but was still quite far from that eventuality when I discovered Dr. Sarno and started doing the work (the Structured Educational Program, plus Claire Weekes for anxiety). My belief was instant, because for many decades I'd understood the mindbody connection and believed in the power of self-healing - I just hadn't put it all together with my lifetime of anxiety and previously mild symptoms, plus this totally new idea of emotional repression. Dr. Sarno did that for me. As I said, I dropped the balance clinic immediately, along with the clinic owner's theory that I was a migrainer, and I also stopped seeing an "alternative" MD who was attempting to do cranio-sacral work on me. I doubled down on my workouts with an age-appropriate physical trainer (I was 60 at that time) with a goal of less fear and more determination to restore my strength and activity. Which I totally did. Until the pandemic shutdowns in early 2020, but that's another story, and it's 100% stress-related. Living in today's dysfunctional world doesn't make any of this easy, folks.Anyway, I'm just wanting to know if people think this kind of physiotherapy (one that aims to retrain the brain, instead of build muscle, etc.) can help?
I thought you might be interested in this video. David in this success story mentions that he was diagnosed with FND. He suffered all manner of symptoms for around 8 years and he recovered by doing TMS work.It is looking more and more to me like FND is the same as TMS
You don't need to pay a lot of money to do this kind of work. Looking back on my experience with one of the worst manifestations of TMS, which is CRPS, I know that if I had examples of people who recovered and who told me that I just must go through the right steps, I could have done it at the cost of a few books. My TMS therapist was great except she was out of network, but I could have done it without her if only I had more confidence that somebody else with CRPS had succeeded.I just saw this post. I am currently dealing with this diagnosis. Someone else I know with FND told me “it just gets worse over time.” I was very discouraged by this. I am hoping doing the work will help me. I currently have it lined up to do a form of PT that is neuroscience based. But of course, it’s out of network.
That is a sweeping across-the-board statement that is simply not true. If you research it you will see that some people diagnosed with FND get worse, some stay the same, some get completely better, some get partially better. You would be doing yourself a big favour to adopt the mindset and attitude of that you will be one of the ones who will get better. The ones who don't get better are more likely to be those who don't have or don't endeavour to foster that kind of mindset or don't do mind/body work in order to get better. Don't listen to negative prognosis comments, start to make your brain feel safe! -- Watch the video I posted above, if you haven't already done so, and seek out other positive stories while you get stuck into doing mind/body work. Good luck on your journey to recovery.Someone else I know with FND told me “it just gets worse over time.”
Any exercise
You don't need to pay a lot of money to do this kind of work. Looking back on my experience with one of the worst manifestations of TMS, which is CRPS, I know that if I had examples of people who recovered and who told me that I just must go through the right steps, I could have done it at the cost of a few books. My TMS therapist was great except she was out of network, but I could have done it without her if only I had more confidence that somebody else with CRPS had succeeded.
That is a sweeping across-the-board statement that is simply not true. If you research it you will see that some people diagnosed with FND get worse, some stay the same, some get completely better, some get partially better. You would be doing yourself a big favour to adopt the mindset and attitude of that you will be one of the ones who will get better. The ones who don't get better are more likely to be those who don't have or don't endeavour to foster that kind of mindset or don't do mind/body work in order to get better. Don't listen to negative prognosis comments, start to make your brain feel safe! -- Watch the video I posted above, if you haven't already done so, and seek out other positive stories while you get stuck into doing mind/body work. Good luck on your journey to recovery.
Thanks! I will go back and read it throughly.